• Decrease font size
  • Return font size to normal
  • Increase font size
U.S. Department of Health and Human Services

MAUDE - Manufacturer and User Facility Device Experience

  • Print
  • Share
  • E-mail
-
Super Search Devices@FDA
510(k) | DeNovo | Registration & Listing | Adverse Events | Recalls | PMA | HDE | Classification | Standards
CFR Title 21 | Radiation-Emitting Products | X-Ray Assembler | Medsun Reports | CLIA | TPLC
 

 
 
8 records meeting your search criteria returned- Product Code: DRE Product Problem: Retraction Problem Report Date From: 01/1/2009
New Searchexport reports to excelExport to Excel | HelpHelp
ManufacturerBrand NameDate Report Received
BAYLIS MEDICAL COMPANY INC. VERSACROSS CONNECT LAAC ACCESS SOLUTION 10/16/2023
THE SPECTRANETICS CORPORATION SPECTRANETICS TIGHTRAIL ROTATING DILATOR 06/25/2020
THE SPECTRANETICS CORPORATION SPECTRANETICS TIGHTRAIL SUB-C ROTATING D 01/17/2020
THE SPECTRANETICS CORPORATION SPECTRANETICS TIGHTRAIL ROTATING DILATOR 03/04/2019
THE SPECTRANETICS CORPORATION TIGHTRAIL ROTATING DILATOR SHEATH 11/05/2018
SPECTRANETICS SPECTRANETICS TIGHTRAIL ROTATING DILATOR 07/07/2017
SPECTRANETICS SPECTRANETICS 13F TIGHTRAIL ROTATING SHE 05/31/2017
SPECTRANETICS TIGHTRAIL ROTATING DILATOR SHEATH 03/25/2016
-
-